Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tetrahydrofuran → 5-Chloro-3-hydroxy-3-(3-methoxyphenyl)-1,3-dihydro-2H-indol-2-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | 3-Bromoanisole | HCID 16971 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 5-chloro-1H-indole-2,3-dione | HCID 87203 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 생성물 | 5-Chloro-3-hydroxy-3-(3-methoxyphenyl)-1,3-dihydro-2H-indol-2-one | HCID 22560825 | — |
| 생성물 | HCID 178490745 | HCID 178490745 | — |
반응 단계
A solution of 3-methoxyphenylmagnesium bromide is prepared from 3.5 g of magnesium in 10 ml of THF and from a solution of 25 g of 1-bromo-3-methoxy-benzene in 40 ml of THF. This solution is added dropwise, under a nitrogen atmosphere, to a mixture of 8 g of 5-chloro-1H-indole-2,3-dione in 50 ml of THF, while keeping the temperature of the reaction medium below 40° C., followed by refluxing for 1 hour. The reaction mixture is cooled to RT, poured into saturated NH4Cl solution and extracted with EtOAc, the organic phase is washed with water and dried over Na2SO4, and the solvent is evaporated off under vacuum. 9.1 g of the expected product are obtained after crystallization from hot iso ether; m.p.=212° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07425566B2 |
| 출처 데이터셋 | uspto-grants-2008_09 |
| ORD ID | ord-1935a5b414384453ae3b0fd32dff8349 |
| 출처 메모 | uspto-grants-2008_09 |